Canonical Allele Identifier: CA4183006
Gene: DNAH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2739424
ClinVar RCV Id: RCV003535330
dbSNP Id: rs370585539
ExAC: 7:21920314 T / C
gnomAD v2: 7-21920314-T-C
gnomAD v3: 7-21880696-T-C
gnomAD v4: 7-21880696-T-C
MyVariant Identifiers: chr7:g.21920314T>C (hg19) chr7:g.21880696T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21880696T>C , CM000669.2:g.21880696T>C GRCh38
NC_000007.13:g.21920314T>C , CM000669.1:g.21920314T>C GRCh37
NC_000007.12:g.21886839T>C NCBI36
NG_012886.2:g.342482T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000409508.8:c.12196-6T>C MANE Select ENSP00000475939.1:n.12196-6T>C
ENST00000328843.10:c.12217-6T>C ENSP00000330671.7:n.12217-6T>C
ENST00000409508.7:c.12196-6T>C ENSP00000475939.1:n.12196-6T>C
ENST00000620169.4:c.12217-6T>C ENSP00000481693.1:n.12217-6T>C
NM_001277115.1:c.12196-6T>C NP_001264044.1:n.12196-6T>C
NM_001277115.2:c.12196-6T>C MANE Select NP_001264044.1:n.12196-6T>C
Search 100 bp 5'
Search 100 bp 3'